This paper is in the following e-collection/theme issue:

Clinical Informatics (1112) Personal Health Records, Patient-Accessible Electronic Health Records, Patient Portals (620) Clinical Information and Decision Making (1570) Adoption and Change Management of eHealth Systems (774) Electronic Health Records (1132) Quality Improvement (269) Health Care Quality and Health Services Research (284) Consumer & Patient Education and Shared-Decision Making (745) Participatory Medicine & E-Patients (822) Patient Engagement and Empowerment (42) Patient-Clinician Relationship (19)

Published on in Vol 27 (2025)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/62670, first published .
Electronic Health Record Data Collection Practices to Advance Standardization and Interoperability of Patient Preferences for Interpretation Services: Qualitative Study

Electronic Health Record Data Collection Practices to Advance Standardization and Interoperability of Patient Preferences for Interpretation Services: Qualitative Study

Electronic Health Record Data Collection Practices to Advance Standardization and Interoperability of Patient Preferences for Interpretation Services: Qualitative Study

Authors of this article:

Krysta Heaney-Huls1 Author Orcid Image ;   Rida Shams1 Author Orcid Image ;   Ruth Nwefo1 Author Orcid Image ;   Rachel Kane2 Author Orcid Image ;   Janna Gordon3 Author Orcid Image ;   Alison M Laffan1 Author Orcid Image ;   Scott Stare4 Author Orcid Image ;   Prashila Dullabh1 Author Orcid Image
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